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灵芝酸A增强抗氧化作用并保护线粒体膜,且降低无镁培养基中原代海马神经元的凋亡率。

Ganoderic acid A potentiates the antioxidant effect and protection of mitochondrial membranes and reduces the apoptosis rate in primary hippocampal neurons in magnesium free medium.

作者信息

Jiang Z M, Qiu H B, Wang S Q, Guo J, Yang Z W, Zhou S B

出版信息

Pharmazie. 2018 Feb 1;73(2):87-91. doi: 10.1691/ph.2018.7108.

Abstract

Ganoderma lucidum extracts have shown antiepileptic effects in in vivo and in vitro studies. In this work, primary hippocampal neurons cultured in magnesium-free medium were used to study the neuroprotective effects of ganoderic acid A and B (GA-A and GA-B) on superoxide dismutase (SOD) activity and mitochondrial membrane potential, to improve our understanding of their antiepileptic effect. The activity of SOD was determined by the xanthine oxidase assay, the variations of mitochondrial membrane potential and cell apoptosis were measured by JC-1 fluorescent staining and flow cytometry. It was found that the SOD activity and mitochondrial membrane potential (118.84 U/mg protein and 244.08 Δψm) of the epileptic hippocampal neurons were significantly lower than control values (135.95 U/mg protein and 409.81 Δψm), associated with an increase of cell apoptosis (31.88% vs. 8.84%). These circumstances can be improved by treatment of GA-A/GA-B (for SOD, 127.15±3.82 / 120.52±4.30 U/mg protein; for membrane potential (Δψm), 372.35 / 347.28; and for cell apoptosis (%), 14.93 / 20.52). Results indicated that GA-A significantly improved SOD activity, while both GA-A/GA-B tranquillized the mitochondrial membrane potential of hippocampal neurons, and thereby protected these neurons by inhibiting apoptosis.

摘要

灵芝提取物在体内和体外研究中均显示出抗癫痫作用。在本研究中,使用在无镁培养基中培养的原代海马神经元来研究灵芝酸A和B(GA-A和GA-B)对超氧化物歧化酶(SOD)活性和线粒体膜电位的神经保护作用,以增进我们对其抗癫痫作用的理解。通过黄嘌呤氧化酶法测定SOD活性,通过JC-1荧光染色和流式细胞术测量线粒体膜电位变化和细胞凋亡情况。结果发现,癫痫海马神经元的SOD活性和线粒体膜电位(分别为118.84 U/mg蛋白和244.08 Δψm)显著低于对照值(分别为135.95 U/mg蛋白和409.81 Δψm),同时细胞凋亡增加(31.88% 对8.84%)。而GA-A/GA-B处理可改善这些情况(对于SOD,分别为127.15±3.82 / 120.52±4.30 U/mg蛋白;对于膜电位(Δψm),分别为372.35 / 347.28;对于细胞凋亡(%),分别为14.93 / 20.52)。结果表明,GA-A显著提高了SOD活性,而GA-A/GA-B均稳定了海马神经元的线粒体膜电位,从而通过抑制凋亡来保护这些神经元。

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